Canonical Allele Identifier: CA469545845
Gene: PCDH15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.55566435C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.53806675C>T , CM000672.2:g.53806675C>T GRCh38
NC_000010.10:g.55566435C>T , CM000672.1:g.55566435C>T GRCh37
NC_000010.9:g.55236441C>T NCBI36
NG_009191.2:g.999617G>A
NG_009191.3:g.1827508G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642496.1:c.3986G>A
ENST00000644397.2:c.5127G>A MANE Select ENSP00000495195.1:p.Glu1709=
ENST00000373965.6:c.4938G>A ENSP00000363076.3:p.Glu1646=
ENST00000414778.5:c.4935G>A ENSP00000410304.2:p.Glu1645=
ENST00000495484.5:c.1155G>A ENSP00000480780.1:p.Glu385=
ENST00000614895.4:c.4950G>A ENSP00000478512.1:p.Glu1650=
ENST00000616114.4:c.4932G>A ENSP00000483745.1:p.Glu1644=
ENST00000618301.4:c.1287G>A ENSP00000482780.1:p.Glu429=
ENST00000621708.4:c.4953G>A ENSP00000484454.1:p.Glu1651=
NM_001142771.1:c.4953G>A NP_001136243.1:p.Glu1651=
NM_001142772.1:c.4938G>A NP_001136244.1:p.Glu1646=
NM_001354420.1:c.4932G>A NP_001341349.1:p.Glu1644=
NM_001354429.1:c.5061G>A NP_001341358.1:p.Glu1687=
XR_001747192.2:n.11419G>A
XR_001747193.2:n.11410G>A
NM_001142771.2:c.4953G>A NP_001136243.1:p.Glu1651=
NM_001142772.2:c.4938G>A NP_001136244.1:p.Glu1646=
NM_001354420.2:c.4932G>A NP_001341349.1:p.Glu1644=
NM_001354429.2:c.5061G>A NP_001341358.1:p.Glu1687=
NM_001384140.1:c.5127G>A MANE Select NP_001371069.1:p.Glu1709=